A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5679719



Internal ID21706040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172212231..172212231hg38UCSC Ensembl
chr1:172181371..172181371hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17183706
Samples
Known GenesDNM3
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5679719
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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